Fully human targeted cytotoxic fusion proteins: new anticancer agents on the horizon
- PMID: 22593247
Fully human targeted cytotoxic fusion proteins: new anticancer agents on the horizon
Abstract
Cytotoxic fusion proteins for tumor therapy are composed of an antibody-based targeting moiety and an effector molecule. Effectors may possess enzymatic activity confering cytoxicity after internalization or be an antibody-targeted death-receptor ligand that induces apoptosis after interaction with a death receptor. In this review, we focus on cytotoxic fusion proteins which, in most cases, are composed of fully human targeting and effector moieties. Regarding the first category, as outlined above, we focus on fusion proteins based on ribonucleases, granzyme B, apoptosis-inducing factor and death-associated protein kinases. The second category of fusion proteins makes use of cell-death inducing ligands such as tumor-necrosis factor, tumor necrosis factor α-related, apoptosis-inducing ligand fas ligand and a tumor-targeting antibody moiety. For the latter category, prodrug-related concepts are also covered. The critical issues to be resolved for improved efficacy and safety are discussed.
Similar articles
-
Target cell-restricted apoptosis induction of acute leukemic T cells by a recombinant tumor necrosis factor-related apoptosis-inducing ligand fusion protein with specificity for human CD7.Cancer Res. 2005 Apr 15;65(8):3380-8. doi: 10.1158/0008-5472.CAN-04-2756. Cancer Res. 2005. PMID: 15833872
-
Granzyme M as a novel effector molecule for human cytolytic fusion proteins: CD64-specific cytotoxicity of Gm-H22(scFv) against leukemic cells.Cancer Lett. 2013 Dec 1;341(2):178-85. doi: 10.1016/j.canlet.2013.08.005. Epub 2013 Aug 22. Cancer Lett. 2013. PMID: 23973499
-
A bispecific enediyne-energized fusion protein containing ligand-based and antibody-based oligopeptides against epidermal growth factor receptor and human epidermal growth factor receptor 2 shows potent antitumor activity.Clin Cancer Res. 2010 Apr 1;16(7):2085-94. doi: 10.1158/1078-0432.CCR-09-2699. Epub 2010 Mar 23. Clin Cancer Res. 2010. PMID: 20332319
-
Targeted cancer therapy: conferring specificity to cytotoxic drugs.Acc Chem Res. 2008 Jan;41(1):98-107. doi: 10.1021/ar700108g. Epub 2007 Aug 18. Acc Chem Res. 2008. PMID: 17705444 Review.
-
Human toxin-based recombinant immunotoxins/chimeric proteins as a drug delivery system for targeted treatment of human diseases.Expert Opin Drug Deliv. 2011 May;8(5):605-21. doi: 10.1517/17425247.2011.566269. Epub 2011 Apr 1. Expert Opin Drug Deliv. 2011. PMID: 21453191 Review.
Cited by
-
Development of a human immuno-oncology therapeutic agent targeting HER2: targeted delivery of granzyme B.J Exp Clin Cancer Res. 2019 Jul 30;38(1):332. doi: 10.1186/s13046-019-1333-6. J Exp Clin Cancer Res. 2019. PMID: 31362764 Free PMC article.
-
Generation of an artificial human B cell line test system using Transpo-mAbTM technology to evaluate the therapeutic efficacy of novel antigen-specific fusion proteins.PLoS One. 2017 Jul 13;12(7):e0180305. doi: 10.1371/journal.pone.0180305. eCollection 2017. PLoS One. 2017. PMID: 28704435 Free PMC article.
-
Advances in epidermal growth factor receptor specific immunotherapy: lessons to be learned from armed antibodies.Oncotarget. 2020 Sep 22;11(38):3531-3557. doi: 10.18632/oncotarget.27730. eCollection 2020 Sep 22. Oncotarget. 2020. PMID: 33014289 Free PMC article. Review.
-
Novel angiogenin mutants with increased cytotoxicity enhance the depletion of pro-inflammatory macrophages and leukemia cells ex vivo.Cancer Immunol Immunother. 2015 Dec;64(12):1575-86. doi: 10.1007/s00262-015-1763-8. Epub 2015 Oct 15. Cancer Immunol Immunother. 2015. PMID: 26472728 Free PMC article.
-
Targeted human cytolytic fusion proteins at the cutting edge: harnessing the apoptosis-inducing properties of human enzymes for the selective elimination of tumor cells.Oncotarget. 2019 Jan 25;10(8):897-915. doi: 10.18632/oncotarget.26618. eCollection 2019 Jan 25. Oncotarget. 2019. PMID: 30783518 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous